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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238834Generated: October 31, 2026

Anisole → Methyl 6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/2238834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantMethyl 6-(4-methoxybenzyloxy)nicotinateHCID 23144104—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 6-oxo-1,6-dihydropyridine-3-carboxylateHCID 41634389.3%

Reaction Steps

Methyl 6-(4-methoxybenzyloxy)nicotinate (2.66 g, 9.73 mmol) obtained in Step 2 and anisole (10.6 mL) were dissolved in trifluoroacetic acid (15 mL), followed by stirring at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and saturated sodium hydrogencarbonate was added to the resulting residue, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The precipitated solid was collected by filtration to afford methyl 2-oxo-1,2-dihydropyridine-5-carboxylate (1.33 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718808B2
Source datasetuspto-grants-2010_05
ORD IDord-a503ed07ef6f41eba717cf2d1df86b47
Source noteuspto-grants-2010_05